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Cited by 347

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

Enantioselective Nitroaldol Reaction of α-Ketoesters Catalyzed by Cinchona Alkaloids

Open access
Li, Hongming, Wang, Baomin, Deng, Li·2006·Journal of the American Chemical Society

Abstract

The development of highly enantioselective and general catalytic nitroaldol (Henry) reactions with ketones is a challenging yet desirable task in organic synthesis. In this communication, we report an asymmetric nitroaldol reaction with alpha-ketoesters catalyzed by a new C6'-OH cinchona alkaloid catalyst. This is the first highly efficient organocatalytic asymmetric Henry reaction with ketones. This reaction is operationally simple and affords high enantioselectivity as well as good to excellent yield for a broad range of alpha-ketoesters.

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Crossref · 10.1021/ja057237l

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Metadata

Authors
Li, H., Wang, B., & Deng, L.
Venue
Journal of the American Chemical Society
Published
2005-12-22
Volume
128
Issue
3
Pages
732-733
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2025243710
Cited by
347
References
9
FWCI
14.29
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Enantioselective Nitroaldol Reaction of α-Ketoesters Catalyzed by Cinchona Alkaloids. https://app.cochat.ai/papers/10.1021/ja057237l
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Li, H., Wang, B., & Deng, L. (2006). Enantioselective Nitroaldol Reaction of α-Ketoesters Catalyzed by Cinchona Alkaloids. Journal of the American Chemical Society. https://doi.org/10.1021/ja057237l

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.